P
US9522183B2ActiveUtilityPatentIndex 87

Compositions and methods for inducing immune tolerance

Assignee: PAULSON JAMES CPriority: Jul 31, 2010Filed: Jul 29, 2011Granted: Dec 20, 2016
Est. expiryJul 31, 2030(~4.1 yrs left)· nominal 20-yr term from priority
Inventors:PAULSON JAMES CMACAULEY MATTHEWNEMAZEE DAVID
A61P 35/00A61K 2039/55555A61K 39/35A61K 39/001A61K 47/6911A61K 39/0008A61K 9/127A61P 29/00A61K 39/385A61K 47/48815A61K 2039/5158A61K 2039/5154
87
PatentIndex Score
19
Cited by
43
References
7
Claims

Abstract

The present invention provides liposomal compositions for inducing immune tolerance. The compounds typically comprise a liposome displaying a specific antigen and also a binding moiety for a sialic acid binding Ig-like lectin (Siglec)expressed on B cells. The invention also provides methods for inducing tolerance to a protein or polypeptide antigen (e.g., a protein antigen) in a subject. The methods involve administering to the subject a pharmaceutical composition that co-presents both the antigen and a glycan ligand for a Siglec expressed on B lymphocytes.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for reducing antigen-specific antibodies to a polypeptide antigen in a subject, comprising administering to the subject a pharmaceutical composition comprising a liposome; a CD22, Siglec G, or Siglec-10 glycan ligand; and an effective amount of a T cell-dependent MHC class II, B cell-specific polypeptide antigen that is linked to a lipid and co-displayed on the liposome with the CD22, Siglec G, or Siglec-10 glycan ligand; to thereby reduce production of antibodies to the antigen by B cells in the subject. 
     
     
       2. The method of  claim 1 , wherein the antigen is an autoantigenan or an alloantigen. 
     
     
       3. The method of  claim 1 , wherein the subject is a human. 
     
     
       4. The method of  claim 3 , wherein the Siglec ligand is 9-N-biphenylcarboxyl-NeuAcα2-6Galβ1-4GlcNAc (6′-BPCNeuAc), NeuAcα2-6Galβ1-4GlcNAc, or NeuAcα2-6Galβ1-4(6-sulfo)GlcNAc. 
     
     
       5. The method of  claim 1 , wherein the polypeptide antigen is a self-antigen, an autoantigen, an alloantigen, a food antigen, or a tissue specific antigen. 
     
     
       6. The method of  claim 1 , wherein the polypeptide antigen is a foreign antigen. 
     
     
       7. The method of  claim 1 , wherein the administering is parenteral administration.

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